Evidence map›Paper›PMID 41017291›Full record

ArticleJournal of the American Geriatrics Society2025

Use of Drugs With Actionable Pharmacogenetic Biomarkers and Possible Prescribing Changes Among Older People.

Zinan Zhao, Yuxuan Zhao, Xiaowen Hu, Xue Wang, Gengchen Wang, Xinyi Zhang, Wenliang Dong, Luwen Shi, Xiaodong Guan, Christine Y Lu and 2 more

Abstract read
In one paragraph

Article in Journal of the American Geriatrics Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Zinan ZhaoDepartment of Pharmacy, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing Key Laboratory of Assessment of Clinical Drugs Risk and Individual Application (Beijing Hospital), Beijing 100730, P.R. China.
Yuxuan ZhaoSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.
Xiaowen HuSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.
Xue WangSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.
Gengchen WangSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.
Xinyi ZhangSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.
Wenliang DongSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.
Luwen ShiSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.
Xiaodong GuanSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.ORCID 0000-0002-1290-3827
Christine Y LuDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.
Pengfei JinDepartment of Pharmacy, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing Key Laboratory of Assessment of Clinical Drugs Risk and Individual Application (Beijing Hospital), Beijing 100730, P.R. China.
Xiaoyan NieSchool of Pharmaceutical Sciences, Peking University Health Science Center, Beijing, China.ORCID 0000-0002-1443-2176

Funding

National Natural Science Foundation of China 72374011
6 · The paper itself

Abstract

backgroundPharmacogenetic testing offers a pathway to safer prescribing and improved outcomes in older adults, who face heightened risks of adverse drug reactions due to polypharmacy and age-related metabolic changes. This study evaluates the prevalence of actionable pharmacogenetic biomarker use and estimates the potential impact of genotype-guided dosing in Chinese older adults.

methodsThis retrospective cross-sectional analysis utilized 2015-2017 claims data from the China Health Insurance Research Association (CHIRA), encompassing 3,309,025 older patients (≥ 65 years) and 74,415,484 prescriptions. Drugs with Clinical Pharmacogenomics Implementation Consortium (CPIC) Level A evidence for actionable pharmacogenetic variants (n = 53) were identified. Key measures included the prescribing prevalence of Level A drugs and projected rates of actionable phenotype-driven dosing changes, calculated using population-specific genotype frequencies from PharmGKB and published sources.

resultsAmong older adults, 43.4% (433.8 per 1000) were prescribed ≥ 1 CPIC Level A drug. Atorvastatin (131.1 per 1000), omeprazole (124.3 per 1000), and clopidogrel (75.7 per 1000) were the most common. Over one-third (36.5%; 365.3 per 1000) of exposures required genotype-guided dose adjustments, with clopidogrel (CYP2C19) and statins (SLCO1B1) representing the highest-priority gene-drug interactions (259.6 and 221.8 per 1000, respectively).

conclusionsCPIC Level A pharmacogenetic biomarkers are prevalent in Chinese older adults, with over 40% exposed to actionable gene-drug pairs and 36.5% requiring dose adjustments. These findings highlight the clinical imperative to integrate pharmacogenetic testing into geriatric care, prioritize CYP2C19 and SLCO1B1 testing, and develop region-specific guidelines to mitigate polypharmacy risks. Policymakers and clinicians should consider targeted implementation strategies to optimize prescribing safety and efficacy in aging populations.

Indexed as

PharmacogeneticsPharmacogenomic TestingPractice Patterns, Physicians'AgedAged, 80 and overBiomarkersChinaCross-Sectional StudiesCytochrome P-450 CYP2C19FemaleGenotypeHumansLiver-Specific Organic Anion Transporter 1MalePolypharmacyRetrospective StudiesBiomarkersCytochrome P-450 CYP2C19Liver-Specific Organic Anion Transporter 1clinical impactgeriatricindividualized medicinepharmacogenetic

Identifiers

PMID41017291
PMCPMC12748018

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.